Canonical Allele Identifier: CA2672898854

Gene: CYP4V2 KLKB1

Linked Data

• gnomAD v4: 4-186211284-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186211290del , CM000666.2:g.186211290del	GRCh38
NC_000004.11:g.187132444del , CM000666.1:g.187132444del	GRCh37
NC_000004.10:g.187369438del	NCBI36
NG_007965.1:g.24771del
NG_012095.2:g.7312del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.*649del (CYP4V2) MANE Select	ENSP00000368079.4:n.*649del
ENST00000502665.1:n.1462del (CYP4V2)
ENST00000507209.5:n.6925del (CYP4V2)
ENST00000511608.5:c.201+2018del (KLKB1)
NM_207352.3:c.*649del (CYP4V2)	NP_997235.3:n.*649del
XM_005262935.2:c.*649del (CYP4V2)	XP_005262992.1:n.*649del
XM_006714184.2:c.*649del (CYP4V2)	XP_006714247.1:n.*649del
XM_011531931.1:c.-3419del (KLKB1)	XP_011530233.1:n.-3419del
XM_011531932.1:c.-3669del (KLKB1)	XP_011530234.1:n.-3669del
XM_011531933.1:c.-3483del (KLKB1)	XP_011530235.1:n.-3483del
XM_005262935.4:c.*649del (CYP4V2)	XP_005262992.1:n.*649del
XM_017008037.1:c.*649del (CYP4V2)	XP_016863526.1:n.*649del
NM_207352.4:c.*649del (CYP4V2) MANE Select	NP_997235.3:n.*649del